Pressure related hysteresis manipulation in a pressurized flow system

ABSTRACT

Exemplary embodiments of the present disclosure are directed to manipulating pressure-related hysteresis in a pressurized flow system by setting the pressure of the system to a predetermined location in the hysteresis band to advantageously minimize an effect of the pressure related hysteresis on the pressure of the system or to advantageously benefit from the effects of the hysteresis on the pressure of the system.

This application is a Continuation of Application U.S. patentapplication Ser. No. 14/381,978 filed on Aug. 28, 2014 which is aNational Stage Application of International Application No.PCT/US2013/029539, filed Mar. 7, 2013, which claims priority to U.S.Provisional Application No. 61/607,910, filing date Mar. 7, 2012. Eachof the foregoing applications are incorporated herein by reference inits entirety.

RELATED APPLICATIONS

This application claims priority to U.S. Provisional Application No.61/607,910, filing date Mar. 7, 2012, which is incorporated herein byreference in its entirety.

FIELD OF THE TECHNOLOGY

In general, the technology of the present disclosure is directed tomethods, processes, systems, and computer readable instructions forcontrolling pressurization in a pressurized flow system, such as, forexample a CO₂-based chromatography or a CO₂-based extraction system. Inparticular, the technology of the present disclosure is directed tomanipulation of pressure-related hysteresis in a pressurized flow systemto advantageous minimize or benefit from pressure-related hysteresiseffects on the system.

BACKGROUND

Chromatographic techniques are important tools for the identificationand separation of complex samples. The basic principle underlyingchromatographic techniques is the separation of a mixture intoindividual components by transporting the mixture in a moving fluidthrough a retentive media. The moving fluid is typically referred to asthe mobile phase and the retentive media is typically referred to as thestationary phase. The separation of the various constituents of themixture is based on differential partitioning between the mobile andstationary phases. Differences in components' partition coefficientresult in differential retention on the stationary phase, resulting inseparation.

Conventionally, the methods of choice for chromatographic separationshave been gas chromatography (GC) and liquid chromatography (LC). Onemajor difference between GC and LC is that the mobile phase in GC is agas, whereas the mobile phase in LC is a liquid. For example, in GC, asupply of inert carrier gas (mobile phase) is continually passed as astream through a heated column containing porous sorptive media(stationary phase). A sample of the subject mixture is injected into themobile phase stream and passed through the column, where separation ofthe mixture is primarily due to the differences in the volatilecharacteristics of each sample component at the temperature of thecolumn. A detector, positioned at the outlet end of the column, detectseach of the separated components as they exit the column. Although GC istypically a sensitive method of analysis, the high temperatures requiredin GC make this method unsuitable for high molecular weight biopolymersor proteins (heat will denature them), frequently encountered inbiochemistry.

Conversely, LC is a separation technique in which the mobile phase is aliquid and does not require volatilization of the sample. Liquidchromatography that generally utilizes small packing particles andmoderately high pressure is referred to as high-performance liquidchromatography (HPLC); whereas liquid chromatography that generallyutilizes very small packing particles and high pressure is referred toas ultra-high performance liquid chromatography (UHPLC). In HPLC andUHPLC the sample is forced by a liquid at high pressure (the mobilephase) through a column that is packed with a stationary phase composedof irregularly or spherically shaped particles, a porous monolithiclayer, or a porous membrane.

Because LC uses liquid as the mobile phase, LC techniques are capable ofanalyzing higher molecular weight compounds and, in some cases, LC canbe used to prepare large scale batches of purified protein(s). However,in contrast, GC techniques are typically more sensitive and readilyallow for the separation of single chiral materials. Thus, GC hasconventionally been used to isolate and determine the relative purity ofa chiral compound, e.g., by determining the enantiomeric excess (% ee)or the diastereomeric excess (% de) of a particular sample. As with mostchromatographic techniques, the limiting factor in both GC and LC hasbeen the ability to obtain and/or reproduce pure sample separations,each of which are typically dependent on the apparatus, methods, andconditions employed, e.g., flow rate, column size, column packingmaterial, solvent gradient, etc.

Supercritical Fluid Chromatography is another chromatographic technique,which has typically been used in preparative applications. For everyliquid substance there is a temperature above which it can no longerexist as a liquid, no matter how much pressure is applied. Likewise,there is a pressure above which the substance can no longer exist as agas no matter how much the temperature is raised. These points arecalled the supercritical temperature and supercritical pressure, anddefine the boundaries on a phase diagram for a pure substance (FIG. 1).At this point, the liquid and vapor have the same density and the fluidcannot be liquefied by increasing the pressure. Above this point, whereno phase change occurs, the substance acts as a supercritical fluid(SF). Thus, SF can be described as a fluid obtained by heating above thecritical temperature and compressing above the critical pressure. Thereis a continuous transition from liquid to SF by increasing temperatureat constant pressure or from gas to SF by increasing pressure atconstant temperature.

The term SFC, while typically standing for Supercritical FluidChromatography, does not require or mean that supercritical conditionsare obtained during or maintained throughout the separation. That is,columns do not have to be always operated in the critical region of themobile phase. For example, in the event that the mobile phase includes amodifier (e.g., CO₂ and methanol as a modifier), the mobile phase isoften in its subcritical region (e.g., a highly compressed gas or acompressible liquid rather than a supercritical fluid). In fact, asGuiochon et al note in section 2.3 of their review article entitled“Fundamental challenges and opportunities for preparative supercriticalfluid chromatography” Journal of Chromatography A, 1218 (2011)1037-1114: “It is obvious that SFC has very often been and still is rununder subcritical conditions.” Thus, the term SFC is not limited toprocesses requiring supercritical conditions.

Because SFC typically uses CO₂, SFC processes are inexpensive,innocuous, eco-friendly, and non-toxic. There is typically no need forthe use of volatile solvent(s) (e.g., hexane). Finally, the mobile phasein SFC processes (e.g., CO₂ together with any modifier/additive as a SF,highly compressed gas, or compressible liquid) typically have higherdiffusion constants and lower viscosities relative to liquid solvents.The low viscosity means that pressure drops across the column for agiven flow rate is greatly reduced. The increased diffusivity meanslonger column length can be used.

SUMMARY

Exemplary embodiments of the present disclosure are directed methods,apparatuses, systems, and computer readable storage mediums configuredto manipulate pressure-related hysteresis in a pressurized flow systemby setting the pressure of the system to a predetermined location in thehysteresis band to advantageously minimize an effect of the pressurerelated hysteresis on the pressure of the system or to advantageouslybenefit from the effects of the hysteresis on the pressure of thesystem. Embodiments of the pressurized flow system can be implemented asa CO₂-based chromatography system in which a mobile phase is passedthrough a stationary phase, sample components of a sample in the mobilephase are separated, and one or more characteristics of the samplecomponents are detected.

In one embodiment, a pressurized flow system having pressure relatedhysteresis is disclosed. The system includes a valve and a processingdevice. The valve is configured to adjust the pressure of the system.The controller is in communication with the valve to adjust the pressureof the system to a predetermined location with respect to a pressurerelated hysteresis band.

In another embodiment, a method of manipulating pressure-relatedhysteresis in a pressurized flow system is disclosed. The methodincludes pressurizing the system and adjusting a pressure of the systemby a first quantity that exceeds a pressure range associated with apressure related hysteresis band to set the pressure to a firstpredetermined location in the hysteresis band.

In another embodiment, a non-transitory computer readable storage mediumstores instructions to be executed by a processing device is disclosed.Execution of the instructions causes the processing device to shift apressure related hysteresis band by a first quantity in response to afirst command signal, shift the pressure related hysteresis band by asecond quantity after a predetermined time period elapsed in which adisturbance to the pressure of the system occurred. The second quantityexceeding the pressure range associated with the hysteresis band to setthe pressure of the system to an upper boundary of the hysteresis band.Execution of the instructions by the processing device can further causethe processing device to increase the pressure of the system based on apredetermined gradient.

In some embodiments, the valve can be controlled to adjust the pressureby a quantity that exceeds a pressure range associated with thehysteresis band to shift the hysteresis band and to set the pressure ofthe system at a predetermined location in the hysteresis band. Thepressure range associated with the hysteresis band can have an upperboundary and a lower boundary, and the valve can be controlled to adjustthe pressure to be greater than the upper boundary or less than thelower boundary. In some embodiments, the pressure range associated withthe hysteresis band can be substantially constant so that when thehysteresis band is shifted, the upper boundary and lower boundary shiftby a substantially identical pressure value.

In some embodiments, the valve to adjust the pressure of the system to ahigher pressure to exceed the upper boundary of the pressure range andto shift the upper boundary of the hysteresis band to the higherpressure.

In some embodiments, the valve can be adjusted to adjust the pressure ofthe system to a lower pressure to reduce the pressure of the systembeyond the lower boundary of the pressure range and to shift the lowerboundary of the hysteresis band to the lower pressure.

In some embodiments, the valve can be controlled to reduce the pressureof the system from a first pressure value that is greater than the lowerboundary to a second pressure value that is less than the lower boundaryto shift the hysteresis band so that the lower boundary is substantiallyequal to the second pressure value.

In some embodiments, the valve can be controlled to increase thepressure of the system from the second pressure value to a thirdpressure value that is greater than the upper boundary to shift thehysteresis band so that the upper boundary is substantially equal to thethird pressure value. The first and third pressure values can besubstantially equal.

In some embodiments, the valve can be controlled to transition from thesecond pressure value to the third pressure value after a predeterminedtime period has elapsed.

In some embodiments, the valve can be adjusted to set the pressure to atleast one of an upper boundary, a lower boundary, and a center of thehysteresis band.

In some embodiments, the pressure is set at an upper boundary of thehysteresis band and to an initial pressure value associated with apressure gradient before a sample is injected into the system.

In some embodiments, the pressure is decreased to shift the upperboundary of the hysteresis band to pre-injection pressure value that isless than the initial pressure value, the sample is injected into thesystem, the pressure is set at the upper boundary of the hysteresis bandand to the initial pressure value after the injection, and the pressureof the system is increase according to the pressure gradient from theinitial pressure value.

In some embodiments, the valve is controlled using a decaying periodicsignal having converging upper and lower peaks. The upper boundary ofthe hysteresis band can shift to the pressure set by the upper peaks andthe lower boundary of the hysteresis band can shift to the pressure setby the lower peaks in an alternating sequence until a peak-to-peakamplitude of the periodic signal decays to be less than the pressurerange of the hysteresis band. The pressure of the system can bepositioned approximately at a center of the hysteresis band after thepeak-to-peak amplitude of the periodic signal decays to be less than thepressure range.

In some embodiments, the valve comprises an actuator in communicationwith a valve member and the actuator adjusts a position of the valvemember to adjust the pressure of the system. In some embodiments, theactuator and valve member comprises a dynamic pressure regulator of thesystem.

In some embodiments, the actuator can be a solenoid and/or a voice coil.

In some embodiments, the valve in response to a command signal.

In some embodiments, the system can be a CO₂-based chromatographysystem.

One or more embodiments feature methods or processes directed toproviding improved control over pressure in a pressurized flow system.For example, in an embodiment, the methods or processes provide improvedpressure control for a back pressure regulator in a CO₂-basedchromatographic system. In particular the methods or processes providean advantage of controlling a location in the hysteresis band in theback pressure regulator to improve “takeoff” or initial/responsebehavior at the beginning of a pressure gradient and performance ofisobaric runs. Any combination or permutation of embodiments isenvisioned.

BRIEF DESCRIPTION OF THE DRAWINGS

The foregoing and other features and advantages provided by the presentdisclosure will be more fully understood from the following descriptionof exemplary embodiments when read together with the accompanyingdrawings, in which:

FIG. 1 is an exemplary graph of the physical state of a substance inrelation to a temperature and pressure associated with the substance;

FIG. 2 is a block diagram of an exemplary pressurized flow system;

FIG. 3 is a block diagram of an exemplary arrangement of an embodimentof the system of FIG. 2;

FIG. 4 is a block diagram of another exemplary arrangement of anembodiment of the system of FIG. 2;

FIG. 5 is a flow diagram of a mobile phase through a system managerportion of the an exemplary embodiment of the pressurized flow system;

FIG. 6 is a cross-sectional view of a valve assembly for an exemplarydynamic pressure regulator in an exemplary embodiment of the pressurizedsystem;

FIG. 7 is a block diagram of an exemplary control system that can beimplemented to control an operation of an exemplary embodiment of thepressurized flow system;

FIG. 8 shows a graph that illustrates an exemplary technique fordetermining an effect of pressure-related hysteresis in an exemplaryembodiment of the pressurized flow system;

FIG. 9 shows a graph that illustrates another exemplary technique fordetermining an effect of pressure-related hysteresis in an exemplaryembodiment of the pressurized flow system;

FIG. 10 shows a graph that illustrates yet another exemplary techniquefor determining an effect of pressure-related hysteresis in an exemplaryembodiment of the pressurized flow system;

FIG. 11 shows graphs illustrating an exemplary response of the pressureof an exemplary embodiment the system to adjustments in positions of avalve member of an exemplary dynamic pressure regulator;

FIG. 12 shows graphs illustrating an exemplary process for controllingan actuator of an exemplary embodiment of the dynamic pressure regulatorto set the pressure of an exemplary embodiment of the pressurized flowsystem to a predetermined location in a hysteresis band;

FIG. 13 shows a graph corresponding to a pressure gradient for exemplarysample runs using the process of FIG. 12; and

FIG. 14 shows graphs illustrating another exemplary process forcontrolling an actuator of an exemplary embodiment of the dynamicpressure regulator to set the pressure of an exemplar embodiment of thepressurized flow system to a predetermined location in the hysteresisband.

DETAILED DESCRIPTION

SFC can be adapted as a hybrid between HPLC and GC apparatuses, wherethe predominant modification is replacement of either the liquid or gasmobile phase with a supercritical fluid (or near supercritical fluid)mobile phase, such as with CO₂. In SFC, the mobile phase is initiallypumped as a liquid or gas and is brought into the supercritical regionby heating or pressurizing the mobile phase above its supercriticaltemperature/pressure prior to entry into a column. As the mobile phasepasses through an injection valve, the sample is introduced into thesupercritical stream, and the mixture is then transferred into a column.The mixture passes through the column (at supercritical or liquid state)and into the detector.

In general, the mobile phase in SFC processes have the ability to actboth as substance carriers (like the mobile phases in GC), and dissolvesubstances readily (like the solvents used in LC). In addition togenerally having lower viscosities and better diffusion profiles similarto those of certain gases, the mobile phase in SFC processes alsogenerally have high densities and dissolving capacities similar to thoseof certain liquids. For example, SFs' high densities (0.2-0.5 gm/cm³)provide for their remarkable ability to dissolve large, non-volatilemolecules, e.g., supercritical or near supercritical CO₂ readilydissolves n-alkanes, di-n-alkyl phthalates, and polycyclic and aromaticcompounds. Since the diffusion of solutes in a SFC mobile phase is aboutten times greater than that in liquids (about three times less than ingases), this results in a decrease in resistance to mass transfer in thecolumn and allows for fast high resolution separation. Also, thesolvation strength of the mobile phase in SFC processes is directlyrelated to the fluid density. Thus, the solubility of solids can beeasily manipulated by making slight changes in temperatures andpressures.

Another important property of the mobile phase in SFC processes is thatit provides high resolution chromatography at much lower temperatures.For example, an analyte dissolved in supercritical CO₂ can be recoveredby reducing the pressure and allowing the sample to evaporate underambient laboratory conditions. This property is useful when dealing withthermally unstable analytes, such as high molecular weight biopolymersor proteins. The combination of one or more mechanical or column changesto an SFC instrument (e.g., a CO₂-based chromatography instrument)coupled with the inherent properties of the SFC itself, allows for theseparation of both chiral and achiral compounds, and has becomeincreasingly predominant in the field of preparatory separations fordrug discovery and development. Despite considerable advances in SFCtechnology, there is a need to develop innovative methods andapparatuses that improve the use of SFC. Controlling and stabilizing thepressure in an SFC instrument by one or more process and/or improvingone or more of the instrumental characteristics of the system, may leadto, amongst others, improved compound separation and efficiency.

For example, better resolution and increased flow rate would decreasecycle times (i.e., shorter cycle times) and allow for improvedseparation of both chiral and achiral compounds, and lead to an overallincrease in laboratory efficiency; increased speed and throughput woulddecrease the amount of solvent and cost(s) associated with SFC; and theability to further integrate SFC with other detection methods, such asMass Spectrometry (MS), Flame Ionization Detectors (FID), andUltraviolet/Visible (UV) detectors, would improve the mainstream use ofSFC using a mobile phase including CO₂ as an eco-friendly, yeteffective, alternative method for the fast, complete, and sensitiveanalysis of analytes.

Exemplary embodiments of the present disclosure are directed tomanipulating pressure-related hysteresis in a pressurized flow system,such as a CO₂-based chromatography system or other pressured flowsystems. Exemplary embodiments, can implement one or more procedures orprocesses for setting the pressure of the system to a predeterminedlocation in the hysteresis band to advantageously minimize the effectsof the hysteresis on the pressure of the system or to advantageouslybenefit from the effects of the hysteresis on the pressure of thesystem. As one example, a sample detection run can be implemented with apressure gradient for which it is advantageous to minimize the effectsof the hysteresis. For such runs, the initial pressure associated withthe pressure gradient can be set to an upper or lower boundary of thehysteresis band. As another example, a sample detection run can beimplemented for which a substantially constant pressure is advantageous.For such runs, the pressure of the system can be set approximately to acenter of the hysteresis band.

As used herein, the terms “downstream” and “upstream” refer to relativelocations in a system flow, wherein upstream refers to being associatedwith an earlier portion of the system flow compared to a later portionof the system flow and downstream refers to being associated with alater portion of the system flow compared to an earlier portion of thesystem flow.

FIG. 2 is a block diagram of an exemplary pressurized flow system, whichin the present embodiment is implemented as a CO₂-based chromatographysystem 10. While the present embodiment is illustrative of a CO₂-basedchromatography system, those skilled in the art will recognize thatexemplary embodiments of the present disclosure can be implemented asother pressurized flow systems and that one or more system components ofthe present disclosure can be implemented as components of otherpressurized systems. The system 10 can be configured to detect samplecomponents of a sample using chromatographic separation in which thesample is introduced into a mobile phase that is passed through astationary phase. The system 10 can include one or more systemcomponents for managing and/or facilitating control of the physicalstate of the mobile phase, control of the pressure of the system 10,introduction of the sample to the mobile phase, separation of the sampleinto components, and/or detection of the sample components, as well asventing of the sample and/or mobile phase from the system 10.

In the present embodiment, the system 10 can include a solvent deliverysystem 12, a sample delivery system 14, a sample separation system 16, adetection system 18 (e.g., PDA detector), and system/convergence manager20. In some embodiments, the system components can be arranged in one ormore stacks. As one example, in one embodiment, the system components ofthe system 10 can be arranged in a single vertical stack (FIG. 3). Asanother example, the system components of the system 10 can be arrangedin multiple stacks (FIG. 4). Those skilled in the art will recognizethat other arrangements of the components of the system 10 are possible.Furthermore, while embodiments of the system 10 have been illustrated asincluding system components 12, 14, 16, 18, and 20, those skilled in theart will recognize that embodiments of the system 10 can be implementedas a single integral unit, that one or more components can be combined,and/or that other configurations are possible.

The solvent delivery system 12 can include one or more pumps 22 a, 22 bconfigured to pump one or more solvents 24, such as mobile phase media23 (e.g., carbon dioxide) and/or modifier media 25 (i.e., a co-solvent,such as e.g., methanol, ethanol, 2-methoxyethanol, isopropyl alcohol, ordioxane), through the system 10 at a predetermined flow rate. Forexample, the pump 22 a can be in pumping communication with the modifiermedia 25 to pump the modifier media 25 through the system 10, and thepump 22 b can be in pumping communication with the mobile phase media 23to pump the mobile phase media 23 through the system 10. An output ofthe pump 22 a can be monitored by a transducer 26 a and an output of thepump 22 b can be monitored by a transducer 26 b. The transducers 26 a,26 b can be configured to sense the pressure and/or flow rate associatedwith the output of the solvent 24 from the pumps 22 a, 22 b,respectively.

The outputs of the pumps 22 a, 22 b can be operatively coupled to aninput of accumulators 28 a and 28 b, respectively. The accumulators 28 aand 28 b are refilled by the outputs of the pumps 22 a and 22 b,respectively, and can contain an algorithm to reduce undesiredfluctuations in the flow rate and/or pressure downstream of the pumps 22a and 22 b, which can cause detection noise and/or analysis errors onthe system 10. An output of the accumulator 28 a can be monitored by atransducer 30 a and an output of the accumulator 28 b can be monitoredby a transducer 30 b. The transducers 30 a, 30 b can be configured tosense pressure and/or flow rate at an output of the accumulators 28 a,28 b, respectively. The outputs of the accumulators 28 a, 28 b can beoperatively coupled to a multiport valve 32, which can be controlled tovent the solvent 24 (e.g., mobile phase media 23 and modifier media 25)being pumped by the pumps 22 a, 22 b and/or to output the solvent 24 toa mixer 34. The mixer 34 can mix the modifier media 25 and the mobilephase media 23 output from the pumps 22 a, 22 b, respectively (e.g.,after first passing through the accumulators 28 a, 28 b) and can outputa mixture of the mobile phase media 23 and the modifier media 25 to forma solvent stream (i.e., mobile phase) that flows through the system 10.The output of the mixer 34 can be operatively coupled to thesystem/convergence manager 20 as discussed in more detail below.

In exemplary embodiments, the solvent delivery system 12 can include amultiport solvent selection valve 36 and/or a degasser 38. The solventselection valve 36 and/or the degasser 38 can be operatively disposedbetween an input of the pump 22 a and solvent sources, e.g., containers40, such that the solvent selection valve 36 and/or the degasser 38 arepositioned upstream of the pump 22 a. The solvent selection valve 36 canbe controlled to select the modifier media 23 to be used by the system10 from one or more solvent containers 40 and the degasser 38 can beconfigured to remove dissolved gases from the media modifier 23 beforethe media modifier 23 is pumped through the system 10.

In exemplary embodiments, the solvent delivery system 12 can include apre-chiller 42 disposed between an input of the pump 22 b and a solventsource, e.g., container 41, such that the pre-chiller is disposedupstream of the input to the pump 22 b and downstream of the solventcontainer 41. The pre-chiller 42 can reduced the temperature of themobile phase media 23 before it is pumped through the system 10 via thepump 22 b. In the present embodiment, the mobile phase media 23 can becarbon dioxide. The pre-chiller can decrease the temperature of thecarbon dioxide so that the carbon dioxide is maintained in a liquidstate (i.e., not a gaseous state) as it is pumped through at least aportion of the system 10. Maintaining the carbon dioxide in a liquidstate can facilitate effective metering of the carbon dioxide throughthe system 10 at the specified flow rate.

The pumps 22 a and 22 b can pump the solvent 24 through the system 10 topressurize the system 10 to a specified pressure, which may becontrolled, at least in part, by the system/convergence manager 20. Inexemplary embodiments, the system 10 can be pressurized to a pressurebetween about 700 psi and about 18,000 psi or about 1,400 psi and about8,000 psi. In one embodiment, the system 10 can be pressurized to apressure of about 6,000 psi. By pressurizing the system 10 at thesepressure levels (such as those pressure levels described above), thesolvent stream (i.e., mobile phase) can be maintained in a liquid statebefore transitioning to a supercritical fluid state or nearsupercritical state (e.g., highly-compressed gas or compressible liquid)for a chromatographic separation in a column, which can be accomplishedby raising the temperature of the pressurized solvent stream.

The sample delivery system 14 can select one or more samples to bepassed through the system 10 for chromatographic separation anddetection. The sample delivery system 14 can include a sample selectionand injection member 44 and a multi-port valve 45. The sample selectionand injection member 44 can include a needle through which the samplecan be injected into the system 10. The multiport valve 45 can beconfigured to operatively couple the sample selection and injectionmember 44 to an input port of the system/convergence manager 20.

The sample separation system 16 can receive the sample to be separatedand detected from the sample delivery system 14, as well as thepressurized solvent stream from the solvent delivery system 12, and canseparate components of the sample passing through the system 10 tofacilitate detection of the samples using the detection system 18. Thesample separation system 16 can include one or more columns 46 disposedbetween an inlet valve 48 and an outlet valve 50. The one or morecolumns 46 can have a generally cylindrical shape that forms a cavity,although one skilled in the art will recognize that other shapes andconfigurations of the one or more columns is possible. The cavity of thecolumns 46 can have a volume that can at least be partially filled withretentive media, such as hydrolyzed silica, such as C₈ or C₁₈, or anyhydrocarbon, to form the stationary phase of the system 10 and topromote separation of the components of the sample. The inlet valve 48can be disposed upstream of the one or more columns can be configured toselect which of the one or more columns 46, if any, receives the sample.The outlet valve 50 can be disposed downstream of the one or morecolumns 46 to selective receive an output from the one or more columns46 and to pass the output of the selected one or more columns 46 to thedetection system 18. The columns 46 can be removeably disposed betweenthe valves 48, 50 to facilitated replacement of the one or more columns46 new columns after use. In some embodiments, multiple sampleseparation systems 16 can be included in the system 10 to provide anexpanded quantity of columns 46 available for use by the system 10 (FIG.4).

In exemplary embodiments, the sample separation system 16 can include aheater 49 to heat the pressurized solvent stream 24 prior and/or whilethe pressured solvent stream 24 passes through the one or more columns46. The heater 49 can heat the pressurized solvent stream to atemperature at which the pressured solvent transition from a liquidstate to a supercritical fluid state so that the pressurized solventstream passes through the one or more columns 46 as a supercriticalfluid.

Referring again to FIG. 2, the detection system 18 can be configured toreceive components separated from a sample by the one or more columns 46and to detect a composition of the components for subsequent analysis.In an exemplary embodiment the detection system 18 can include one ormore detectors 51 configured to sense one of more characteristics of thesample components. For example, in one embodiment, the detectors 51 canbe implemented as one or more photodiode arrays.

The system/convergence manager 20 can be configured to introduce asample from the sample delivery system 14 into the pressurized solventstream flowing from the solvent delivery system 12 and to pass thesolvent stream and sample to the sample separation system 16. In thepresent embodiment, the system/convergence manager 20 can include amultiport auxiliary valve 52 which receives the sample injected by thesample delivery system 14 through a first inlet port and the pressurizedsolvent stream from the solvent delivery system 12 through a secondinlet port. The auxiliary valve 52 can mix the sample and the solventstream and output the sample and solvent stream via an outlet port ofthe multiport auxiliary valve 52 to an inlet port of the inlet valve 48of the sample separation system 16.

The system/convergence manager 20 can also be configured to control thepressure of the system 10 and to facilitate cooling, heating, and/orventing of the solvent from the system 10, and can include a vent valve54, a shut off valve 56, a back pressure regulator 58, and a transducer59. The vent valve 54 can be disposed downstream of the detection system18 can be configured to decompress the system 10 by venting the solventfrom the system 10 after the solvent has passed through the system 10.The shut off valve 56 can be configured to disconnect the solvent supplyfrom the inlet of the pump 22 b of the solvent delivery system toprevent the solvent from being pumped through the system 10.

The back pressure regulator 58 can control the back pressure of thesystem 10 to control the flow of the mobile phase and sample through thecolumn, to maintain the mobile phase in the supercritical fluid state(or, in some embodiments, in a near supercritical state, such as, ahighly-compressed gas or compressible liquid) as the mobile phase passesthrough the one or more columns 46 of the sample separation system 16,and/or to prevent the back pressure from forcing the mobile phasereversing its direction a flow through the one or more columns 46.Embodiments of the back pressure regulator 58 can be configured toregulate the pressure of the system 10 so that the physical state of thesolvent stream (i.e., mobile phase) does not change uncontrollablyupstream of and/or within the back pressure regulator 58. The transducer59 can be a pressure sensor disposed upstream of the back pressureregulator 58 to sense a pressure of the system 10. The transducer 59 canoutput a feedback signal to a processing device which can process thesignal to control an output of an actuator control signal from theprocessing device.

In exemplary embodiments, as shown in FIG. 5, the back pressureregulator 58 can include a dynamic pressure regulator 57, a staticpressure regulator 61, and a heater 63. The static pressure regulator 61can be configured to maintain a predetermined pressure upstream of theback pressure regulator 58. The dynamic pressure regulator 57 can bedisposed upstream of the static pressure regulator 61 and can beconfigured to set the system pressure above the predetermined pressuremaintained by the static regulator 61. The heater 63 can be disposeddownstream of the dynamic pressure regulator 57 and can be disposed inclose proximity to the static pressure regulator 61 to heat the solventstream as it passes through the static pressure regulator 61 to aid incontrol of the physical state of the solvent as it passes through thestatic pressure regulator. The structure, function, and/or operation ofthe back pressure regulator 58, static pressure regulator, and/ordynamic regulator are described in more detail below.

In summary, an exemplary operation of the CO₂-based chromatographysystem 10 can pump mobile phase media 23 and modifier media 25 at aspecified flow rate through the system 10 as a solvent stream (i.e.,mobile phase) and can pressurize the system 10 to a specified pressureso that the solvent stream maintains a liquid state before entering thesample separation system 16. A sample can be injected into thepressurized solvent stream by the sample delivery system 14, and thesample being carried by the pressurized solvent stream can pass throughthe sample separation system 16, which can heat the pressurized solventstream to transition the pressurized solvent stream from a liquid stateto a supercritical fluid state. The sample and the supercritical fluidsolvent stream can pass through at least one of the one or more columns46 in the sample separation system 16 and the column(s) 46 can separatecomponents of the sample from each other. The separated components canpass the separated components to the detection system 18, which candetect one or more characteristics of the sample for subsequentanalysis. After the separated sample and solvent pass through thedetection system 18, the solvent and the sample can be vented from thesystem 10 by the system/convergence manager 20.

In other embodiments, the CO₂-based chromatography system 10 describedherein can also be used for preparatory methods and separations. Typicalparameters, such as those described above, may be manipulated to achieveeffective preparatory separations. For example, the system 10 describedherein confers the benefit of exerting higher flow rates, largercolumns, and column packing size, each of which contributes to achievingpreparatory separation and function, while maintaining little or novariability in overall peak shape, peak size, and/or retention time(s)when compared to respective analytical methods and separations thereof.Thus, in one embodiment, the present disclosure provides CO₂-basedchromatography systems, which are amendable to preparatory methods andseparations with high efficiency and correlation to analytical runs.

FIG. 6 is a cross-sectional view of an exemplary embodiment of a dynamicpressure regulator 57 along a longitudinal axis L of the dynamicpressure regulator. The dynamic pressure regulator 57 can be implementedas a valve assembly that includes a proximal head portion 72, anintermediate body portion 74, and a distal actuator portion 76. The headportion 72 of the valve assembly can include an inlet 78 to receive thepressurized solvent stream and an outlet 80 through which thepressurized solvent stream is output such that the solvent stream flowsthrough the head portion from the inlet 78 to the outlet 80. A seat 82can be disposed within the head portion 72 and can include a bore 84through which the solvent stream can flow from the inlet 78 to theoutlet 80 of the head.

A needle 86 extends into the head portion 72 from the body portion 74 ofthe valve assembly through a seal 88. A position of the needle 86 can becontrolled with respect to the seat 82 to selectively control a flow ofthe solvent stream from the inlet 78 to the outlet 80. In exemplaryembodiments, the position of the needle 86 can be used to restrict theflow through the bore 84 of the seat 82 to increase the pressure of thesystem 10 and can selectively close the valve by fully engaging the seat82 to interrupt the flow between the inlet 78 and the outlet 80. Bycontrolling the flow of the solvent stream through the head portionbased on the position of the needle 86, the pressure of the system 10can be increased or decreased. For example, the pressure of the system10 can generally increase as the needle 86 moves towards the seat 82along the longitudinal axis L and can generally decrease as the needle86 moves away from the seat 82 along the longitudinal axis L.

The actuator portion 76 can include an actuator 90, such as a solenoid,voice coil, and/or any other suitable electromechanical actuationdevice. In the present embodiment, the actuator 90 can be implementedusing a solenoid having a main body 92 and a shaft 94. The shaft 94 canextend along the longitudinal axis L and can engage a distal end of theneedle 86 such that the needle 86 and shaft can form a valve member. Aposition of the shaft 94 can be adjustable with respect to the main body92 along the longitudinal axis L and can be controlled by a coil (notshown) of the main body 92, which generates a magnetic field that isproportional to an electric current passing through the coil and a loadapplied to the shaft. The electric current passing through the coil canbe controlled in response to an actuator control signal received by theactuator 90. In some embodiments, the actuator control signal can be apulse width modulated (PWM) signal and/or the actuator control signalcan be determined, at least in part, by the feedback signal of thepressure transducer 59.

The position of the shaft 94 can be used to move the needle 86 towardsor away from the seat 82 to increase or decrease pressure, respectively.In exemplary embodiments, a position of the shaft 94, and therefore aposition of the needle 86 with respect to the seat 82 can be controlledand/or determined based on an amount of electric current flowing throughthe solenoid. For example, the greater the electrical current the closerto the needle 86 and shaft 94 are from the seat and the lower thepressure is in the system 10. The relationship between a position of theshaft 94 and the electric current flowing through the coil can beestablished through characterization of the actuator 90. The forceimposed by the load on the solenoid can be proportional to the magneticfield. Similarly, the magnetic field can be proportional to the electriccurrent flowing through the coil of the solenoid. For embodiments inwhich the actuator control signal is implemented as a PWM controlsignal, the pressure through the regulator 57 (e.g., force balancebetween needle 86 and shaft 94) can be set by a correlation to the dutycycle of the PWM control signal, e.g., a percentage of the duty cyclecorresponding to an “on” state.

FIG. 7 is a block diagram of an exemplary control system 100 that can beimplemented to control the pressure of the system 10. The control system100 can include a controller 102 in electrical communication with astorage device 104 (e.g., memory and/or other computer-readable storagemediums). The controller 102 can be implemented as a microcontroller,microprocessor, field programmable gate array (FPGA), and/or otherprocessing devices. The storage 104 can be implemented as non-transitorycomputer readable medium including, for example, magnetic storage disks,optical disks, flash or solid state storage, and/or any othernonvolatile or volatile storage medium including random access memory,such as DRAM, SRAM, EDO RAM, MRAM, and the like. The storage 106 canstore information corresponding to the system 10 and/or componentsthereof. The storage 106 can also store instructions that are executableby the controller 102 to control an operation of system 10 including anoperation of the dynamic back pressure regulator 57. The controller 102can also be in communication with one or more of the pumps 22 a, 22 b,one or more of the transducers 26 a, 26 b, 30 a, 30 b, 59, the injectionmember 44, the dynamic pressure regulator 57, input devices 110, and/ora display 112. In this embodiment, the pumps, 22 a, 22 b can beassociated with pump controllers 108 a, 108 b, respectively, and theactuator 90 of the dynamic pressure regulator 57 can be associated withan actuator controller 114.

The controller 102 can receive signals from and/or transmit signals tothe transducers 26 a, 26 b, 30 a, 30 b, 59, the injection member 44, thepump controllers 108 a, 108 b, one or more input devices 110, such as akeyboard, mouse, or other suitable input devices, the display 112, andthe actuator controller 114, and/or other devices, such as othercontrollers (e.g., processing devices), computing devices (e.g., aLaptop, PC, mainframe), networked devices (e.g., servers, databases),and the like, which can be communicatively coupled to the controller 102via, for example, a communication interface 116. In exemplaryembodiments, the controller 102 can process the received signals and cancontrol an operation of the pumps 22 a, 22 b, the injection member 44,and/or the actuator 90 in response to the signals.

In one exemplary embodiment, the controller 102 can output the actuatorcontrol signal to the actuator controller 114 to control a position ofthe valve member (e.g., shaft 94 and needle 86) to adjust the pressureof the system to control an effect that pressure related hysteresis hasan on the system 10 during operation. In exemplary embodiments, thepressure related hysteresis can affect a response rate of the system 10to requested changes in the pressure (e.g., how quickly the pressurechanges from its current value to a requested value). For example, theresponse rate of the system 10 can be decreased by the effects of thehysteresis such that the system 10 can take longer to reach a requestedpressure value than the system 10 normally would if there was nohysteresis in the system 10.

The hysteresis of the system 10 can be associated with a hysteresisband, which refers to a pressure range over which the hysteresis affectsthe system. The hysteresis band can have an upper boundary and a lowerboundary. When the pressure of the system is within the boundaries ofthe hysteresis band, the hysteresis has a greater effect on a responserate of the system to requested pressure changes. As the pressurechanges in the system, the hysteresis band can track the pressurechanges such that the pressure values associated with the hysteresisband generally change to follow the pressure of the system. The responserate of the system for pressure changes can be dependent on where thecurrent pressure is with respect to the hysteresis band as well as themagnitude of the pressure change requested and/or the rate at which thepressure is requested to change. Generally the effects of the hysteresiscan be more significant larger pressure change and higher rates ofchange. The hysteresis of the system 10 can be quantified bycharacterizing the response of the system to pressure changes. Based onthe characterization of the response to pressure changes, the pressurerange associated with the hysteresis band can be determined.

FIGS. 8-10 show graphs 120, 122, 124, respectively, each of which areillustrative of an exemplary characterization of the hysteresis for anembodiment of the system 10. The graph 120 illustrated in FIG. 8corresponds to a measurement of the pressure of the system 10 forchanges in the actuator control signal implemented using pulse widthmodulation to adjust the pressure of the system. The graph 122illustrated in FIG. 9 corresponds to a measurement of the pressure fordifferent requested rates of change for the pressure of the system 10.The graph 124 of FIG. 10 corresponds to a measurement of the pressure ofthe system 10 for different rates of change of the actuator controlsignal implemented using pulse width modulation. The x-axis 126 of thegraphs 120, 122, 124 corresponds to the pressure of the system 10measured in pounds per square inch (psi). The y-axis 128 of FIG. 8corresponds to a duty cycle of a pulse width modulated (PWM) actuatorcontrol signal measured as percentage. The y-axis 130 of FIG. 9corresponds to a rate of change in the pressure measured in psi perminute (psi/min). The y-axis 132 of FIG. 10 corresponds to a rate ofchange in the PWM actuator control signal measured in percent per minute(%/min).

As shown in FIGS. 8-10, a hysteresis band 134 can be identified in eachgraph 120, 122, 124, which, for the present embodiment, has a pressurerange 136 of about 1,600 psi. For the measurements illustrated in FIGS.8-10, the lower boundary 138 of the hysteresis band 134 occurs at about2,000 psi and the upper boundary 140 of the hysteresis band 134 occursat about 3,600 psi. While the pressure range 136 of the hysteresis band134 is generally constant, the pressure values of the lower and upperboundaries 138 and 140, respectively, can change based on a current andprevious pressure of the system 10. Furthermore, while the hysteresisband 134 has been determined to have a pressure range of 1,600 psi forone embodiment of the system 10, those skilled in the art will recognizethat the pressure range 136 of the hysteresis band 134 can be differentfor this or other embodiments of the system 10 and that the pressurerange 136 of the hysteresis band 134 can be determined as described inFIGS. 8-10 or using other techniques.

FIG. 11 shows a graph 150, 152 of an exemplary response of thehysteresis band 134 to changes in pressure resulting from a change inposition of the shaft 94 and needle 86 as shown in graph 152 and inaccordance with exemplary embodiments of the present disclosure. Thex-axis 154 for graphs 150, 152 corresponds to time, the y-axis 156 ofthe graph 150 corresponds to pressure in psi and the y-axis 158 of thegraph 152 corresponds to a distance between the needle 86 and the seat82 of the actuator 90. A decrease in the distance of shaft 94 and needle86 from the seat 82 as shown in graph 152 (e.g., an increase inpressure) and an increase in the distance between the shaft 94 andneedle 86 from the seat 82 (e.g., a decrease in pressure).

The hysteresis band 134 includes the lower boundary 138 and the upperboundary 140 and has the pressure range 136. As shown in graphs 150,152, when the distance between the needle and the seat is decreased to afirst value 160 in response to a control signal received from theprocessing device, the pressure 162 of the system 10 responds to thechange in position of the needle 86 by increasing to a first pressurevalue 164. As the pressure 162 increases, the hysteresis band 134 shiftsto a first pressure location 166 and the pressure values associated withthe lower and upper boundaries 138, 140 increase by a substantiallysimilar amount such that the pressure range of the hysteresis band 134is unchanged, but the pressure values associated with the hysteresisband 134 change. When the distance between the needle and the seat isincreased to a second value 168 in response to the control signal fromthe processing device, the pressure 162 of the system 10 responds to thechange in position of the needle 86 by decreasing to a second pressurevalue 170. As the pressure 162 decreases, the hysteresis band 134 shiftsto a second pressure location 172 and the pressure values associatedwith the lower and upper boundaries 138, 140 decrease by a substantiallysimilar amount such that the pressure range 136 of the hysteresis band134 is unchanged, but the pressure values associated with the hysteresisband 134 change. The rate with which the hysteresis band 134 changes itslocation with respect to the pressure can be based on, for example, amagnitude in the change of pressure, the rate at which the pressurechange is requested, previous pressure values of the system 10, and thelike.

The pressure related hysteresis associated with embodiments of thesystem 10 can adversely affect an operation of the system 10 as well asa detection sample component. As one example, in some embodiments, auser may implement a sample detection method for which the user wishesto detect sample components over a pressure gradient. The user canspecify a rate of change for the pressure to implement the pressuregradient and can program the system 10 to increase or decrease thepressure of the system 10 at the predetermined rate of change after thesample to be detected has been injected into the system 10. If the rateof change in the pressure is affected by the hysteresis, and the userhas not taken into account the effect of the hysteresis, the pressure ofthe system 10 may not respond as the user expected and/or desired. Forexample, there may be an unacceptable error between the actual rate ofchange of the pressure compared to the predetermined rate of change,there may be an unacceptable delay before the pressure increases at thepredetermined rate of change such that there is a tracking error betweenthe actual pressure gradient and the predetermined pressure gradient,and/or there may be other error, undesirable effects, or unacceptableeffects on the pressure of the system as a result of the hysteresis.

In some instances, the pressure related hysteresis associated withembodiments of the CO₂-based chromatography system can be used toadvantageously affect an operation of the CO₂-based chromatographysystem as well as a detection sample component. As one example, in someembodiments, a user may implement a sample detection method for whichthe user wishes to detect sample components over a substantiallyconstant system pressure (e.g., isobaric chromatographic separation).For such methods, the hysteresis of the CO₂-based chromatography systemcan be used to maintain a substantially constant pressure throughout therun.

The adverse effects of the hysteresis can be advantageously minimizedand/or the advantageous effects of the hysteresis can be realized forembodiments of the CO₂-based chromatography system by setting thepressure of the system to a predetermined location in the hysteresisband. Exemplary embodiments of the CO₂-based chromatography system canbe configured to control a position of the needle 86 with respect to theseat in the dynamic pressure regulator to manipulate the pressure of theCO₂-based chromatography system so that the pressure of the CO₂-basedchromatography system is positioned at a predetermined location in thehysteresis band.

FIG. 12 shows graphs 180, 182 illustrating an exemplary process forcontrolling the actuator 90 of the dynamic pressure regulator 57 to setthe pressure to a predetermined location in a hysteresis band 184. Thegraph 180 represents an electrical current 186 being supplied to theactuator 90 over time 181 and the graph 182 represents a pressure 188 ofthe system 10 that corresponds to the electric current 186 beingsupplied to the actuator 90. The pressure 188 of the system 10 and theelectrical current 186 supplied to the actuator 90 can have initialconditions 190, 192, respectively, which can correspond to the pressure188 of the system 10 and the electrical current 186 of supplied to theactuator 90 upon activation of the system 10, after completion of aprevious sample run (e.g., a previous sample detection), or aftercompletion of a system calibration or diagnostic process. In exemplaryembodiments, a change in pressure of the system 10 can exceed a pressurerange 185 of the hysteresis band to adjust a pressure value of thesystem beyond an upper or lower boundary of the hysteresis band 184 toset the pressure to the upper or lower boundary, respectively, of thehysteresis band 184.

At time 194, the relationship between the system pressure 188 and thehysteresis band 184 can be uncertain. A new sample run can be initiatedfor which a sample is to be chromatographically separated while beingexposed to a pressure gradient 187 and the system can be configured tominimize the effect of the hysteresis on the pressure gradient 187 bysetting 10 the system pressure 188 to a predetermined location in thehysteresis band 184. At time 196, the new sample run can be initiatedand the electric current 186 to the actuator can be increased toposition the needle 86 closer to the seat 82 to increase the pressure188 as shown. The pressure 188 can be increased to a pressure value 198at time 200 that is within a predetermined pressure range 202 to apressure value 204 that corresponds to an initial pressure of thepressure gradient 187 for the sample run. The change in pressure to thepressure value 198 can be greater than the pressure range 185 of thehysteresis band 184 and/or can exceed an upper boundary 210 of thehysteresis band 184 to set the pressure of the system at the upperboundary 210 of the hysteresis band 184. The change in pressure over thetime period between the times 196 and 200 can be referred to as a courseequilibrate period. The hysteresis band 184 can shift with the increasein pressure 188 from its initial undetermined location 206 to a firstlocation 208 with respect to pressure. For example, the upper boundary210 of the hysteresis band 184 can shift to the pressure value 198 andthe lower boundary 212 of the hysteresis band 184 can shift by asubstantially similar amount to a first lower boundary pressure value214 such that a pressure range 185 of the hysteresis band 184 remainsgenerally constant. After the pressure 188 has reached the pressurevalue 198, the electric current 186 can be decreased at time 200 toposition the needle 86 further away from the seat 82 to decrease thepressure of the system 10 to a pressure value 221. The change in thepressure of the system from the pressure value 198 to the pressure value221 can exceed the pressure range 185 of the hysteresis band 184 and/orcan exceed the pressure value associated with the lower boundary 212 ofthe hysteresis band. The hysteresis band 184 can shift to a secondlocation 220 with respect to pressure in preparation for setting thepressure 188 approximately to the pressure value 204 pressure. At thesecond location 220, the pressure 188 of the system can be set at thelower boundary 212 of the hysteresis band 184.

Between times 222 and 224, the pressure 188 can be increased to apressure value 226 that is within a predetermined pressure range 228 tothe pressure value 200. The time period between the times 222 and 224can be referred to as a fine equilibrate period because the pressurerange 228 is smaller than the pressure range 202 of the courseequilibrate. For example, the course equilibrate period can set thepressure 188 to within approximately 100 psi of the pressure value 204and the fine equilibrate period can set the pressure to withinapproximately 50 psi of the pressure value 204. The change in thepressure 188 from the pressure value 221 to the pressure value 226 canbe greater than the pressure range 185 of the hysteresis band and/or canexceed the pressure value associated with the upper boundary 210 of thehysteresis band 184. In some embodiments, the pressure value 226 can beless than, substantially equal to, or greater than the pressure value204. In exemplary embodiments, the pressure 188 can be increase after apredetermined time period and/or in response to a command signal. Thehysteresis band 184 can shift with the increase in the pressure 188 fromthe second location 220 to a third location 230 with respect topressure. For example, the upper boundary 210 of the hysteresis band 184can shift to the pressure value 226 (e.g., the pressure 188 of thesystem is set at the upper boundary 210) and the lower boundary 212 ofthe hysteresis band 184 can shift by a substantially similar amount to alower boundary pressure value 232 such that the pressure range 185 ofthe hysteresis band 184 remains generally constant.

Once the pressure 188 is set approximately to the pressure value 204(e.g., the pressure value 226), the system pressure is set to apredetermined location in the hysteresis band (e.g., at the upperboundary of the hysteresis band) and is ready to process a sample. Theinjection of the sample into the solvent stream (e.g., the mobile phase)can create a pressure disturbance in the system 10, which can disruptthe position of the pressure in the hysteresis band and cause sampledetection errors due to the effects of the hysteresis. To prevent orreduce the effect of the disturbance caused by the injection, the system10 can implement an injection procedure to ensure that the pressure 188of the system 10 is at the predetermined location with respect to thehysteresis band 184 after the injection and disturbance from theinjection settles.

In the injection procedure, a pre-injection command signal can be issuedat time 224 in preparation for receiving an injection of the sample. Insome embodiments, the pre-injection command signal can be issued by thecontroller 102 (e.g., a processing device) of the control system 100. Insome embodiments, the pre-injection command signal can be issued by aprocessing device of a computing device that is in communication withthe system 10 (e.g., in communication with the controller 102). Issuanceof the pre-injection command causes the processing device to control theactuator 90 to position the needle 86 away from the seat 82 to decreasethe pressure 188 in preparation for receiving the injection of thesample. The pressure 188 is decrease by an amount that is exceeds thelower boundary 212 of the hysteresis band 184 to shift the hysteresisband 184 so that a pressure value associated with the upper boundary 210is less than the pressure value 204.

After the injection has been received and the pressure disturbanceassociated with the injection has settled, the system 10 pressure can beincreased to set the initial pressure value for the pressure gradient187 to be within the pressure range 228 (e.g., to approximately thepressure value 204) and to set the pressure to the upper boundary 212(e.g., a predetermined location) of the hysteresis band 184. Bydecreasing the pressure before the injection of the sample andsubsequently increasing the pressure after the disturbance from theinjection has settled to within the pressure range 228 of the pressurevalue 200, exemplary embodiments ensure that the pressure is set to theupper boundary of the hysteresis band and that the pressure of thesystem 10 is approximately the pressure value 204 (e.g., within thepressure range 228) before the pressure gradient 187 is implemented.

The system 10 can be configured to increase the pressure after theinjection based an a predetermined time period and/or a post injectioncontrol signal. For example, experiments can be performed to determine aduration of the disturbance introduced to the system after an injectionand the control system can be configured to increase the pressure of thesystem after a predetermined time has elapsed from receiving thepre-injection control signal. For example, exemplary embodiments canwait for approximately two (2) seconds to about ten (10) second orapproximately five (5) seconds or more. The duration of the disturbancecan be measured based on how long the disturbance takes to settle towithin an acceptable pressure range such that the operation of thesystem 10 can perform sample separation and detection withoutsubstantial effects from the disturbance.

By setting the pressure to the upper boundary of the hysteresis band,the system 10 can eliminate or minimize the effect the hysteresis has onthe pressure gradient 187 since the effect of the hysteresis atpressures greater than the upper boundary of the hysteresis band 184 areminimal. Using this approach, the pressure of the system 10 can beconsistently controlled for sample runs in which a pressure gradient 187is used. There can be some tracking error 236 associated between theideal pressure values and the actual pressure values of the pressuregradient 187, but this tracking error can be considered and compensatedby the system 10 since the response of the system to the pressuregradient 187 is consistent for multiple sample runs. While the presentembodiment is illustrative of a positive pressure gradient, thoseskilled in the art will recognize that a similar procedure can beimplemented for a negative pressure gradient by setting the pressure ofthe system 10 to the lower boundary of the hysteresis band.

FIG. 13 shows a graph 240 of the pressure gradient 187 for exemplarysample runs using the above procedure of FIG. 12. The x-axis 244 of thegraph corresponds to time in minutes and the y-axis 246 of the graphcorresponds to pressure in psi. As shown in FIG. 13, the pressuregradient 187 is substantially consistent across different sample runs.As a result, users of the system 10 can obtain consistent samplemeasurements without substantial variations in the pressure gradient 187due to the hysteresis of the system 10 and/or a disturbance from theinjection of the sample.

FIG. 14 shows graphs 250, 252 illustrating another exemplary process forcontrolling the actuator 90 of the dynamic pressure regulator to set thepressure to a predetermined location in the hysteresis band. The graph250 represents an electrical current 254 being supplied to the actuatorover time and the graph 252 represents a pressure 256 of the system 10that corresponds to the electric current 254 being supplied to theactuator 90. In the present embodiment, the electric current 254 can bea periodic decaying signal, such as a decaying sine wave. While adecaying sine wave is illustrated in this embodiment, those skilled inthe art will recognize that other periodic or aperiodic signals havingalternating peaks can be used, e.g., a decaying triangle wave, or otherdecaying signal having alternating peaks. The electric current 254 ofthe actuator 90 can correspond to a position of the needle with respectto the seat such that increasing current 254 moves the needle 86 towardsfrom the seat 82 (e.g., increases pressure) and decreasing current 254moves the needle 86 away from the seat 82 (e.g., decreasing pressure).The pressure 256 of the system can generally correlate to the decayingperiodic electrical current signal 254 such that the pressure 256 of thesystem 10 generally has a decaying periodic waveform 258 that isproportional to the decaying periodic signal of the electric current254.

As shown in FIG. 14, at time 260, the decaying periodic waveform 258generated by the decaying periodic electric current 262 can have apeak-to-peak amplitude 264 that is greater than a pressure range 266 ofa hysteresis band 268 so that a location of the hysteresis band 268initially follows the decaying periodic waveform 258 of the pressure256. For example, the hysteresis band 268 can shift from a firstlocation 270 to a second position 272 with respect to pressure. Thesecond location 272 can correspond to a first peak 274 of the decayingperiodic waveform 258 such that the upper boundary 276 of the hysteresisband 268 is substantial equal to the pressure value associated with thefirst peak 274. As the pressure 256 decreases from the first peak 274 toa second peak 278, the hysteresis band 268 can shift towards the secondpeak 278 to assume a third location 280 at which the lower boundary 282of the hysteresis band 268 is substantially equal to the pressure valueassociated with the second peak 278.

Thus, the hysteresis band 268 can shift between the alternating peaks ofthe decaying periodic waveform 258 of the pressure 256 until thepeak-to-peak amplitude 264 of the decaying periodic waveform 258 is lessthan or equal to the pressure range 266 of the hysteresis band 268, atwhich time (e.g., time 284) the location of the hysteresis band 268remains generally constant. As the decaying periodic waveform 258 of thepressure 256 continues to decay in response to the decaying periodicsignal of the electric current 254, the pressure 256 of the system stayswithin the upper and lower boundaries 276, 282 of the hysteresis band268 and settles approximately at a center 286 of the hysteresis band268. Thus, the present embodiment can be implemented to set the pressureof the system to about the center (e.g., a predetermined location) inthe hysteresis band 268.

In describing exemplary embodiments, specific terminology is used forthe sake of clarity. For purposes of description, each specific term isintended to at least include all technical and functional equivalentsthat operate in a similar manner to accomplish a similar purpose.Additionally, in some instances where a particular exemplary embodimentincludes a plurality of system elements, device components or methodsteps, those elements, components or steps may be replaced with a singleelement, component or step. Likewise, a single element, component orstep may be replaced with a plurality of elements, components or stepsthat serve the same purpose. Moreover, while exemplary embodiments havebeen shown and described with references to particular embodimentsthereof, those of ordinary skill in the art will understand that varioussubstitutions and alterations in form and detail may be made thereinwithout departing from the scope of the invention. Further still, otheraspects, functions and advantages are also within the scope of theinvention.

The invention claimed is:
 1. A method of manipulating pressure-relatedhysteresis in a pressurized flow system, the method comprising:pressurizing the system; and adjusting a pressure of the system by afirst quantity that exceeds a pressure range associated with a pressurerelated hysteresis band to manipulate the hysteresis by shifting thehysteresis band with respect to the pressure and setting the pressure toa first predetermined location in the hysteresis band, wherein thepressurized flow system is a chromatography or extraction system.
 2. Themethod of claim 1, further comprising: adjusting the pressure of thesystem by a second quantity that exceeds the pressure range to shift thehysteresis band with respect to the pressure and set the pressure to asecond predetermined location in the hysteresis band.
 3. The method ofclaim 2, wherein adjusting the pressure by the second quantity occurs apredetermined time after adjusting the pressure by the first quantity.4. The method of claim 2, wherein adjusting the pressure by the firstquantity occurs in response to a first command signal and adjusting thepressure by the second quantity occurs in response to a second commandsignal.
 5. The method of claim 2, further comprising receiving adisturbance in the system after adjusting the pressure by the firstquantity and before adjusting the pressure by the second quantity. 6.The method of claim 2, wherein the second quantity returns the pressureof the system to a value that is substantially equal to the systempressure of the system before adjusting the pressure by the firstquantity, and wherein the pressure of the system after adjusting thesecond quantity is positioned at a different location in the hysteresisband than the pressure of the system before adjusting by the firstquantity.
 7. The method of claim 2, wherein adjusting the pressure bythe first and second quantities is performed in response to peak valuesof a decaying periodic signal.
 8. The method of claim 2, wherein thesecond predetermined location in the hysteresis band is at least one ofan upper boundary of the hysteresis band and a center of the hysteresisband.
 9. The method of claim 2, further comprising adjusting thepressure of the system by a third quantity, wherein adjusting thepressure by the third quantity is substantially unaffected by ahysteresis associated with the hysteresis band.